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311.
Yiu SM Man WL Wang X Lam WW Ng SM Kwong HK Lau KC Lau TC 《Chemical communications (Cambridge, England)》2011,47(14):4159-4161
MnO(4)(-) is activated by BF(3) to undergo intramolecular coupling of two oxo ligands to generate O(2). DFT calculations suggest that there should be a spin intercrossing between the singlet and triplet potential energy surfaces on going from the active intermediate [MnO(2)(OBF(3))(2)](-) to the O···O coupling transition state. 相似文献
312.
With [Ru(p-cymene)Cl(2)](2) as catalyst, diazo-β-ketoanilides would undergo intramolecular carbenoid arene C-H bond functionalization to afford 3-alkylideneoxindoles in up to 92% yields. The reaction occurs under mild conditions and exhibits excellent chemoselectivity. The lack of primary KIE (k(H)/k(D) ~ 1) suggests that the reaction should not proceed by rate-limiting C-H bond cleavage; a mechanism involving cyclopropanation of the arene is proposed. 相似文献
313.
C.N. Li A.B. Djurišić C.Y. Kwong P.T. Lai W.K. Chan S.Y. Liu 《Applied Physics A: Materials Science & Processing》2005,80(2):301-307
We have systematically investigated the influence of UV ozone and acid (HCl) treatments (separate and combined) of the surface of indium tin oxide (ITO) on the ITO parameters and the performance of organic light-emitting diodes (OLEDs) fabricated on the treated substrates. The ITO substrates were characterized by Hall measurements, Seebeck coefficient measurements and surface-probe microscopy. After ITO characterization, two types of devices (ITO/NPB/rubrene/Alq3/LiF/Al and ITO/TPD/rubrene/Alq3/LiF/Al) were fabricated on the differently treated substrates. It was found that in both cases the optimal treatment was HCl followed by UV ozone, which resulted in the lowest turn-on voltage and the highest luminous efficiency. The maximum luminous efficiency in the ITO/NPB/rubrene/Alq3/LiF/Al OLED with HCl followed by UV ozone treatment was 2.15 lm/W compared to 1.46 lm/W with UV ozone treatment only. PACS 81.65Cf; 85.60.Jb 相似文献
314.
We are interested in the oscillatory behavior of solutions of the Emden-Fowler equation y″+a(x)|y|γ−1y=0, γ>1, where a(x) is a positive continuous function on (0,∞). In the special case when the coefficient a(x) is a power of x, i.e. a(x)=xα for some constant α, the value α∗=−(γ+3)/2 plays a critical role: The equation has both oscillatory and nonoscillatory solutions if α>α∗, while all solutions are nonoscillatory if α<α∗. When a(x) is close to the critical exponent, one of the known results is that if a(x)=x−(γ+3)/2log−σ(x), where σ>0, then all solutions are nonoscillatory. In this paper, this result is further extended to include a class of coefficients in which the above condition with log(x) can be replaced by loglog(x), or logloglog(x) and so on. 相似文献
315.
316.
通过KOH活化纸巾制备活性炭纤维, 比表面积高达1388 m2/g. 用制得的活性炭纤维作为吸附剂进行亚甲基蓝吸附实验研究,用Langmuir和Freundlich吸附模型分析实验数据,并研究pH值对活性炭纤维吸附亚甲基蓝影响. 活性炭纤维吸附速率更适于Pseudo-second-order动力学模型,相关系数高达0.998. 整个浓度变化区间Langmuir吸附等温线比Freundlich吸附等温线更适合实验数据. 所制备活性炭纤维对亚甲基蓝最大平衡吸附量为520 mg/g,实验发现,pH值越高活性炭纤维对亚甲基蓝吸附量越大. 相似文献
317.
A.M.C. Dawes D.J. Gauthier S. Schumacher N.H. Kwong R. Binder A.L. Smirl 《Laser \u0026amp; Photonics Reviews》2010,4(2):221-243
We review recent theoretical and experimental efforts toward developing an all‐optical switch based on transverse optical patterns. Transverse optical patterns are formed when counterpropagating laser beams interact with a nonlinear medium. A perturbation, in the form of a weak switch beam injected into the nonlinear medium, controls the orientation of the generated patterns. Each state of the pattern orientation is associated with a state of the switch. That is, information is stored in the orientation state. A realization of this switch using a warm rubidium vapor shows that it can be actuated by as few as 600 ± 40 photons with a response time of 5 µs. Models of nonlinear optical interactions in semiconductor quantum wells and microresonators suggest these systems are also suitable for use as fast all‐optical switches using this same conceptual design, albeit at higher switching powers. 相似文献